233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 (2018)
- Authors:
- Lostal, William
- Urtizberea, J. Andoni
- Richard, Isabelle
- Alonso-Jiménez, Alicia
- Carlier, Robert-Yves
- Carson, Vincent
- Diaz-Manera, Jordi
- Eymard, Bruno
- Fardeau, Michel
- Gourlay, Marie-Laurence
- Guglieri, Michela
- Hogrel, Jean-Yves
- Kullmann, Bruno
- Levy, Jennifer
- Ono, Yasuko
- Prigent, Hélène
- Saenz, Amets
- Semplicini, Claudio
- Vainzof, Mariz
- Vissing, John
- Maggie, Walter
- Lostal, William
- Autor USP: VAINZOF, MARIZ - IB
- Unidade: IB
- DOI: 10.1016/j.nmd.2018.03.010
- Subjects: DISTROFIA MUSCULAR; MUTAÇÃO GENÉTICA; ENZIMAS; AMINOÁCIDOS; ENSAIO CLÍNICO
- Agências de fomento:
- Financiado pela European Neuromuscular (ENMC)
- Finaciado pela Association Française contre les Myopathies (France)
- Financiado pela Deutsche Gesellschaft für Muskelkranke (Germany)
- Financiado pela Muscular Dystrophy UK
- Financiado pela Muskelsvindfonden (Denmark)
- Financiado pela Prinses Beatrix Spierfonds (The Netherlands)
- Financiado pela Schweizerische Stiftung für die Erforschung der Muskelkrankheiten (Switzerland)
- Financiado pela Telethon Foundation (Italy)
- Financiado pela Spierziekten Nederland (The Netherlands)
- Financiado pela Associated members
- Financiado pela Neuromuscular Association (Finland)
- Language: Inglês
- Imprenta:
- Source:
- Título: Neuromuscular Disorders
- ISSN: 0960-3966
- Volume/Número/Paginação/Ano: v. 28, p. 540-549, 2018
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
LOSTAL, William et al. 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017. Neuromuscular Disorders, v. 28, p. 540-549, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2018.03.010. Acesso em: 31 dez. 2025. -
APA
Lostal, W., Urtizberea, J. A., Richard, I., Alonso-Jiménez, A., Carlier, R. -Y., Carson, V., et al. (2018). 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017. Neuromuscular Disorders, 28, 540-549. doi:10.1016/j.nmd.2018.03.010 -
NLM
Lostal W, Urtizberea JA, Richard I, Alonso-Jiménez A, Carlier R-Y, Carson V, Diaz-Manera J, Eymard B, Fardeau M, Gourlay M-L, Guglieri M, Hogrel J-Y, Kullmann B, Levy J, Ono Y, Prigent H, Saenz A, Semplicini C, Vainzof M, Vissing J, Maggie W. 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 [Internet]. Neuromuscular Disorders. 2018 ; 28 540-549.[citado 2025 dez. 31 ] Available from: https://doi.org/10.1016/j.nmd.2018.03.010 -
Vancouver
Lostal W, Urtizberea JA, Richard I, Alonso-Jiménez A, Carlier R-Y, Carson V, Diaz-Manera J, Eymard B, Fardeau M, Gourlay M-L, Guglieri M, Hogrel J-Y, Kullmann B, Levy J, Ono Y, Prigent H, Saenz A, Semplicini C, Vainzof M, Vissing J, Maggie W. 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 [Internet]. Neuromuscular Disorders. 2018 ; 28 540-549.[citado 2025 dez. 31 ] Available from: https://doi.org/10.1016/j.nmd.2018.03.010 - Reviewing large LAMA2 deletions and duplications in congenital muscular dystrophy patients
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Informações sobre o DOI: 10.1016/j.nmd.2018.03.010 (Fonte: oaDOI API)
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